Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Enikő Mihály"'
Publikováno v:
Case Reports in Emergency Medicine, Vol 2018 (2018)
Emergency department (ED) physicians frequently encounter patients presenting with angioedema. Most of these involve histamine-mediated angioedema; however, less common forms of angioedema (bradykinin-mediated) also occur. It is vital physicians corr
Externí odkaz:
https://doaj.org/article/5b7301c18624433b86e136b10ac40375
Autor:
Dumitru Moldovan, Katalin Csép, Noémi Bara, Daniela Dobru, Enikő Mihály, Adina Hutanu, Valentin Nădășan, Gabriella Gábos
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 27, Iss 3, Pp 255-267 (2019)
Background: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) caused by SERPING1 mutations is a rare monogenic disorder characterized by a high frequency of de novo mutations, allelic heterogeneity and populational differences. Geno-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6537e5c611831cbe59a21c4130fb7db0
https://doi.org/10.2478/rrlm-2019-0029
https://doi.org/10.2478/rrlm-2019-0029
Publikováno v:
Case Reports in Emergency Medicine
Case Reports in Emergency Medicine, Vol 2018 (2018)
Case Reports in Emergency Medicine, Vol 2018 (2018)
Emergency department (ED) physicians frequently encounter patients presenting with angioedema. Most of these involve histamine-mediated angioedema; however, less common forms of angioedema (bradykinin-mediated) also occur. It is vital physicians corr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c71f2935284ab0bed12d23c8d87918c7
http://europepmc.org/articles/PMC6217881
http://europepmc.org/articles/PMC6217881
Autor:
Enikő Mihály, Daniela Dobru, Dumitru Moldovan, Valentin Nădășan, Ramona Popa, Cătălin Dumitrache, Noémi Bara, Gabriella Gábos
Publikováno v:
The Lancet. 390:2119-2120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0adcef0027aa2da2f85ecfb438b32ee4
https://doi.org/10.1016/s0140-6736(17)32206-7
https://doi.org/10.1016/s0140-6736(17)32206-7
Autor:
Enikő Mihály, Dumitru Moldovan, Gábor Széplaki, Henriette Farkas, Lilian Varga, George Füst, Beáta Visy, Zsuzsanna Kelemen, Dorottya Csuka
Publikováno v:
Clinical Immunology. 134:354-358
The diagnosis of hereditary angioedema (HAE) is based on complement tests. We studied for the first time the possible association between complement parameters measured at the time of diagnosis and disease severity in 115 patients with HAE. Serum lev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::798a75578e7d4eb321ff029ded37ecb1
https://doi.org/10.1016/j.clim.2009.11.002
https://doi.org/10.1016/j.clim.2009.11.002
Publikováno v:
Alergologia. 2:65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1eab0cef474c730f6fb4cd127801b4f7
https://doi.org/10.26416/aler.2.2.2018.1687
https://doi.org/10.26416/aler.2.2.2018.1687
Publikováno v:
Iranian Journal of Immunology, Vol 17, Iss 3, Pp 226-235 (2020)
Background: Hereditary angioedema (HAE) is a rare genetic potentially life-threatening disease characterized by episodic non-pruritic subcutaneous and submucosal edema attacks in different parts of the body. Objective: To assess the status of Romania
Externí odkaz:
https://doaj.org/article/013242b4066e4ecaa4af9451488b7484